Phosphatidylserine NEW

Phosphatidylserine (PS) is a crucial glycerophospholipid, a major component of cell membranes, particularly concentrated in the inner leaflet of the plasma membrane in eukaryotic cells. Its chemical structure defines its properties and functions:

Core Structure:

• sn-1 position: Typically a saturated fatty acid (e.g., stearic acid, 18:0).

• sn-2 position: Typically an unsaturated fatty acid (e.g., oleic acid 18:1, arachidonic acid 20:4). The specific fatty acids vary, influencing membrane fluidity.

• Glycerol Backbone: A 3-carbon molecule (sn-glycerol-3-phosphate).

• Two Fatty Acyl Chains: Esterified to the sn-1 and sn-2 hydroxyl groups of the glycerol backbone. These are hydrophobic "tails".

• Phosphate Group: Attached to the sn-3 hydroxyl group of glycerol via a phosphodiester bond. This forms the "linker".

• Serine Headgroup: The amino acid L-serine is attached via a phosphodiester bond to the phosphate group. This is the hydrophilic, polar "head".

  Chemical Formula:

• The general formula for a PS molecule with specific fatty acids is C₄₂H₈₂NO₁₀P (for 1-stearoyl-2-oleoyl-PS, a common form).

• The core structure without specifying fatty acids is often represented as C₃H₈NO₁₀P (for the headgroup + glycerol + phosphate), but this ignores the variable fatty acid chains.

  Key Chemical Features:

• The phosphate group (pKa ~2-3) is fully deprotonated (PO₄²⁻).

• The carboxyl group of serine (pKa ~4.5) is deprotonated (COO⁻).

• The amino group of serine (pKa ~9-10) is protonated (NH₃⁺).

• This gives the PS headgroup a net charge of -1 (PO₄⁻ + COO⁻ + NH₃⁺ = -1 overall). It's a highly negatively charged (anionic) phospholipid.

• Amphipathic: Combines hydrophobic tails (fatty acids) and a hydrophilic head (phosphate + serine). This is essential for forming lipid bilayers.

• Chiral Center: The carbon at position 2 of the glycerol backbone (sn-2 carbon) is chiral. Naturally occurring PS uses the sn-glycerol-3-phosphate configuration.

• Anionic Headgroup: At physiological pH (~7.4):

  Biological Significance (Driven by Chemistry):

• Apoptosis (Programmed Cell Death): Signals phagocytes to engulf the dying cell.

• Blood Clotting: Provides a surface for coagulation factor complexes.

• Membrane Asymmetry: Its concentration on the inner leaflet is maintained by specific enzymes (flippases). Loss of this asymmetry (exposure of PS on the outer leaflet) is a key signal for processes like:

• Protein Recruitment: Its negative charge attracts and activates numerous proteins with polybasic domains (e.g., protein kinase C (PKC), Raf-1, K-Ras, synaptotagmin).

• Cell Signaling: Involved in activating key signaling pathways (e.g., Akt/PKB, MAPK).

• Membrane Fusion: Important in processes like neurotransmitter release at synapses.

Summary Structure:

O

||

O - P - O - CH₂ - CH - COO⁻

|      |          |

O⁻     O⁻        ⁺NH₃

       |

       Glycerol Backbone (C1 & C2 esterified to Fatty Acid Chains)

       / \

      /   \

     R1    R2  (Hydrophobic Fatty Acid Tails)

• O=P-O-: Phosphate Group

• -CH₂-CH-COO⁻: Serine Headgroup (L-Serine)
  ⁺NH₃

• Glycerol Backbone: The central 3-carbon chain.

• R1 & R2: Long hydrocarbon chains of the fatty acids (e.g., -C₁₇H₃₅ for stearate, -C₁₇H₃₃ for oleate).

Phosphatidylserine's unique chemical structure, particularly its serine headgroup and resulting negative charge, underpins its vital roles in membrane biology, signaling, and cellular recognition.